Why you hire for this job?

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As I have experience of 1 years as clinical research coordinator.

With my background in clinical research and current experience at Seven Hills Hospital as a CRC and I have previously worked in IATRIS (TDM LAB) as data entry operator.
I am enthusiastic about the opportunity to contribute to your esteemed organization.

In my role at Seven Hills Hospital,

1. Coordinate and oversee the day-to-day operations of clinical trials.
2. Assist Pl in recruiting, screening, and enrolling study participants.
3. Assist Pl in obtaining informed consent from study participants.
4. Schedule and conduct participant visits and follow-ups.
5. Collect and record accurate data in accordance with the study protocol.
6. Ensure compliance with study protocols, Good Clinical Practice (GCP) guidelines, and regulatory requirements.
7. Maintain study documentation and ensure data integrity.
8. Assist in preparing EC dossier for EC submission.
9. Communicate effectively with study CRO, sponsors, investigators, EC and other stakeholders.
10. Monitor study progress and report any issues or deviations from the protocol to the study sponsor or principal investigator.
11. Participate in site visits, audits, and inspections as required.
12. Provide regular updates and reports to the clinical research team and management.

I am confident that my background, combined with my passion for clinical research, makes me a strong candidate for this position.

Why you hire for this job?

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